全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

DNA Barcoding for Minor Crops and Food Traceability

DOI: 10.1155/2014/831875

Full-Text   Cite this paper   Add to My Lib

Abstract:

This outlook paper addresses the problem of the traceability of minor crops. These kinds of cultivations consist in a large number of plants locally distributed with a modest production in terms of cultivated acreage and quantity of final product. Because of globalization, the diffusion of minor crops is increasing due to their benefit for human health or their use as food supplements. Such a phenomenon implies a major risk for species substitution or uncontrolled admixture of manufactured plant products with severe consequences for the health of consumers. The need for a reliable identification system is therefore essential to evaluate the quality and provenance of minor agricultural products. DNA-based techniques can help in achieving this mission. In particular, the DNA barcoding approach has gained a role of primary importance thanks to its universality and versatility. Here, we present the advantages in the use of DNA barcoding for the characterization and traceability of minor crops based on our previous or ongoing studies at the ZooPlantLab (Milan, Italy). We also discuss how DNA barcoding may potentially be transferred from the laboratory to the food supply chain, from field to table. 1. DNA Barcoding for Plant Identification Plants as primary producers are the basis of human nutrition from time immemorial. It is estimated that about 7,000 species of plants have been cultivated for consumption in human history (FAO data) and a large number of cultivars and varieties are also recognized. The Commission on Genetic Resources for Food and Agriculture (http://www.fao.org/nr/cgrfa/cthemes/plants/en/) estimated that 30 crops are usually referred currently as major agricultural products since they provide 95% of human food energy needs (e.g., rice, wheat, maize, and potato). These resources are widely monitored and well characterized with the analysis of DNA markers specifically developed for each cultivar (see, e.g., [1–3]). On the contrary, reliable characterization tools for the minor varieties are far from being defined. Minor crops include plants for food, pharmaceutical, cosmetic, and ornamental purposes with a modest production in terms of cultivated acreage and quantity of final product [4]. There are no fixed standard values to define a minor crop; however, conventionally, all the local varieties could be placed in this category. Most of these species or varieties show peculiar traits from the alimentary, pharmaceutical, or ornamental points of view. Some examples of minor crops that are now widely cultivated and worldwide distributed are Goji

References

[1]  J. S. C. Smith, E. C. L. Chin, H. Shu et al., “An evaluation of the utility of SSR loci as molecular markers in maize (Zea mays L.): comparisons with data from RFLPS and pedigree,” Theoretical and Applied Genetics, vol. 95, no. 1-2, pp. 163–173, 1997.
[2]  F. De Mattia, G. Lovicu, J. Tardaguila et al., “Genetic relationships between Sardinian and Spanish viticulture: the case of “Cannonau” and ‘Garnacha’,” Journal of Horticultural Science and Biotechnology, vol. 84, no. 1, pp. 65–71, 2009.
[3]  S. R. McCouch, K. Zhao, M. Wright et al., “Development of genome-wide SNP assays for rice,” Breeding Science, vol. 60, no. 5, pp. 524–535, 2010.
[4]  J. Womach, Agriculture: A Glossary of Terms, Programs, and Laws, Congressional Research Service, Library of Congress, Washington, DC, USA, 2005.
[5]  H. Amagase and N. R. Farnsworth, “A review of botanical characteristics, phytochemistry, clinical relevance in efficacy and safety of Lycium barbarum fruit (Goji),” Food Research International, vol. 44, no. 7, pp. 1702–1717, 2011.
[6]  S. E. Kulling and H. M. Rawel, “Chokeberry (Aronia melanocarpa)-a review on the characteristic components and potential health effects,” Planta Medica, vol. 74, no. 13, pp. 1625–1634, 2008.
[7]  J. M. Urpí, J. C. Weber, and C. R. Clement, Peach Palm, Bactris Gasipaes Kunth, vol. 20, Bioversity international, Rome, Italy, 1997.
[8]  S. Ketema, Tef-Eragrostis tef (Zucc.), vol. 12, Bioversity international, Rome, Italy, 1997.
[9]  M. Camciuc, M. Deplagne, G. Vilarem, and A. Gaset, “Okra—Abelmoschus esculentus L. (Moench.) a crop with economic potential for set aside acreage in France,” Industrial Crops and Products, vol. 7, no. 2-3, pp. 257–264, 1998.
[10]  K. T. Moe, S. Kwon, and Y. Park, “Trends in genomics and molecular marker systems for the development of some underutilized crops,” Genes and Genomics, vol. 34, no. 5, pp. 451–466, 2012.
[11]  E. Ernst, “The efficacy of herbal medicine-an overview,” Fundamental and Clinical Pharmacology, vol. 19, no. 4, pp. 405–409, 2005.
[12]  H. A. Tindle, R. B. Davis, R. S. Phillips, and D. M. Eisenberg, “Trends in use of complementary and alternative medicine by us adults: 1997–2002,” Alternative Therapies in Health and Medicine, vol. 11, no. 1, pp. 42–49, 2005.
[13]  G. Heubl, “New aspects of DNA-based authentication of Chinese medicinal plants by molecular biological techniques,” Planta Medica, vol. 76, no. 17, pp. 1963–1974, 2010.
[14]  L. Cornara, B. Borghesi, C. Canali et al., “Smart drugs: green shuttle or real drug?” International Journal of Legal Medicine, vol. 127, no. 6, pp. 1109–1123, 2013.
[15]  I. Bruni, F. De Mattia, A. Galimberti et al., “Identification of poisonous plants by DNA barcoding approach,” International Journal of Legal Medicine, vol. 124, no. 6, pp. 595–603, 2010.
[16]  S. L. Taylor and J. L. Baumert, “Cross-contamination of foods and implications for food allergic patients,” Current Allergy and Asthma Reports, vol. 10, no. 4, pp. 265–270, 2010.
[17]  Z. P. Zeng and J. G. Jiang, “Analysis of the adverse reactions induced by natural product-derived drugs,” British Journal of Pharmacology, vol. 159, no. 7, pp. 1374–1391, 2010.
[18]  J. Costa, I. Mafra, J. S. Amaral, and M. B. P. P. Oliveira, “Detection of genetically modified soybean DNA in refined vegetable oils,” European Food Research and Technology, vol. 230, no. 6, pp. 915–923, 2010.
[19]  S. Babaei, M. Talebi, and M. Bahar, “Developing an SCAR and ITS reliable multiplex PCR-based assay forsafflower adulterant detection in saffron samples,” Food Control, vol. 35, no. 1, pp. 323–328, 2014.
[20]  Y. J. Park, J. K. Lee, and N. S. Kim, “Simple sequence repeat polymorphisms (SSRPs) for evaluation of molecular diversity and germplasm classification of minor crops,” Molecules, vol. 14, no. 11, pp. 4546–4569, 2009.
[21]  S. Soares, I. Mafra, J. S. Amaral, and M. B. P. P. Oliveira, “A PCR assay to detect trace amounts of soybean in meat sausages,” International Journal of Food Science and Technology, vol. 45, no. 12, pp. 2581–2588, 2010.
[22]  F. De Mattia, I. Bruni, A. Galimberti, F. Cattaneo, M. Casiraghi, and M. Labra, “A comparative study of different DNA barcoding markers for the identification of some members of Lamiacaea,” Food Research International, vol. 44, no. 3, pp. 693–702, 2011.
[23]  A. K. Lockley and R. G. Bardsley, “DNA-based methods for food authentication,” Trends in Food Science and Technology, vol. 11, no. 2, pp. 67–77, 2000.
[24]  I. Mafra, I. M. Ferreira, and M. B. P. Oliveira, “Food authentication by PCR-based methods,” European Food Research and Technology, vol. 227, no. 3, pp. 649–665, 2008.
[25]  J. Novak, S. Grausgruber-Gr?ger, and B. Lukas, “DNA-based authentication of plant extracts,” Food Research International, vol. 40, no. 3, pp. 388–392, 2007.
[26]  M. Labra, M. Miele, B. Ledda, F. Grassi, M. Mazzei, and F. Sala, “Morphological characterization, essential oil composition and DNA genotyping of Ocimum basilicum L. cultivars,” Plant Science, vol. 167, no. 4, pp. 725–731, 2004.
[27]  M. Woolfe and S. Primrose, “Food forensics: using DNA technology to combat misdescription and fraud,” Trends in Biotechnology, vol. 22, no. 5, pp. 222–226, 2004.
[28]  S. Imazio, M. Labra, F. Grassi, A. Scienza, and O. Failla, “Chloroplast microsatellites to investigate the origin of grapevine,” Genetic Resources and Crop Evolution, vol. 53, no. 5, pp. 1003–1011, 2006.
[29]  F. De Mattia, F. Grassi, S. Imazio, and M. Labra, “Chloroplast and nuclear DNA markers to characterize cultivated and spontaneous Ribes,” Plant Biosystems, vol. 142, no. 2, pp. 204–212, 2008.
[30]  P. Kumar, V. K. Gupta, A. K. Misra, D. R. Modi, and B. K. Pandey, “Potential of molecular markers in plant biotechnology,” Plant Omics: Journal of Plant Molecular Biology & Omics, vol. 2, no. 4, pp. 141–162, 2009.
[31]  A. Galimberti, F. De Mattia, A. Losa et al., “DNA barcoding as a new tool for food traceability,” Food Research International, vol. 50, no. 1, pp. 55–63, 2013.
[32]  H. Chuang, H. Lur, K. Hwu, and M. Chang, “Authentication of domestic Taiwan rice varieties based on fingerprinting analysis of microsatellite DNA markers,” Botanical Studies, vol. 52, no. 4, pp. 393–405, 2011.
[33]  P. D. Hebert, S. Ratnasingham, and J. R. de Waard, “Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species,” Proceedings of the Royal Society B: Biological Sciences, vol. 270, supplement 1, pp. S96–S99, 2003.
[34]  M. Casiraghi, M. Labra, E. Ferri, A. Galimberti, and F. de Mattia, “DNA barcoding: a six-question tour to improve users' awareness about the method,” Briefings in Bioinformatics, vol. 11, no. 4, Article ID bbq003, pp. 440–453, 2010.
[35]  J. Shaw, E. B. Lickey, E. E. Schilling, and R. L. Small, “Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the Tortoise and the hare III,” American Journal of Botany, vol. 94, no. 3, pp. 275–288, 2007.
[36]  A. J. Fazekas, K. S. Burgess, P. R. Kesanakurti et al., “Multiple multilocus DNA barcodes from the plastid genome discriminate plant species equally well,” PLoS ONE, vol. 3, no. 7, Article ID e2802, 2008.
[37]  A. J. Fazekas, P. R. Kesanakurti, K. S. Burgess et al., “Are plant species inherently harder to discriminate than animal species using DNA barcoding markers?” Molecular Ecology Resources, vol. 9, no. 1, pp. 130–139, 2009.
[38]  D. Mathew, “Biotechnology,” in Horticulture: Methods and Applications, K. V. Peter, Ed., chapter 2, pp. 25–50, New India Publishing Agency, New delhi, India, 1st edition, 2014.
[39]  M. L. Hollingsworth, A. Andra Clark, L. L. Forrest et al., “Selecting barcoding loci for plants: evaluation of seven candidate loci with species-level sampling in three divergent groups of land plants,” Molecular Ecology Resources, vol. 9, no. 2, pp. 439–457, 2009.
[40]  P. M. Hollingsworth, S. W. Graham, and D. P. Little, “Choosing and using a plant DNA barcode,” PLoS ONE, vol. 6, no. 5, Article ID e19254, 2011.
[41]  I. Bruni, F. De Mattia, S. Martellos et al., “DNA barcoding as an effective tool in improving a digital plant identification system: a case study for the area of Mt. Valerio, Trieste (NE Italy),” PloS one, vol. 7, no. 9, Article ID e43256, 2012.
[42]  W. J. Kress, D. L. Erickson, N. G. Swenson, J. Thompson, M. Uriarte, and J. K. Zimmerman, “Advances in the use of DNA barcodes to build a community phylogeny for tropical trees in a puerto rican forest dynamics plot,” PLoS ONE, vol. 5, no. 11, Article ID e15409, 2010.
[43]  S. Federici, A. Galimberti, F. Bartolucci et al., “DNA barcoding to analyse taxonomically complex groups in plants: the case of Thymus (Lamiaceae),” Botanical Journal of the Linnean Society, vol. 171, no. 4, pp. 687–699, 2013.
[44]  A. Gismondi, F. Fanali, J. M. M. Labarga, M. G. Caiola, and A. Canini, “Crocus sativus L. genomics and different DNA barcode applications,” Plant Systematics and Evolution, vol. 299, no. 10, pp. 1859–1863, 2013.
[45]  S. Theodoridis, A. Stefanaki, M. Tezcan, C. Aki, S. Kokkini, and K. E. Vlachonasios, “DNA barcoding in native plants of the Labiatae (Lamiaceae) family from Chios Island (Greece) and the adjacent ?e?me-Karaburun Peninsula (Turkey),” Molecular Ecology Resources, vol. 12, no. 4, pp. 620–633, 2012.
[46]  M. Kojoma, K. Kurihara, K. Yamada, S. Sekita, M. Satake, and O. Iida, “Genetic identification of cinnamon (Cinnamomum spp.) based on the trnL-trnF chloroplast DNA,” Planta Medica, vol. 68, no. 1, pp. 94–96, 2002.
[47]  M. Wang, H. Zhao, L. Wang et al., “Potential use of DNA barcoding for the identification of Salvia based on cpDNA and nrDNA sequences,” Gene, vol. 528, no. 2, pp. 206–215, 2013.
[48]  I. Ganopoulos, P. Madesis, N. Darzentas, A. Argiriou, and A. Tsaftaris, “Barcode High Resolution Melting (Bar-HRM) analysis for detection and quantification of PDO “fava Santorinis” (Lathyrus clymenum) adulterants,” Food Chemistry, vol. 133, no. 2, pp. 505–512, 2012.
[49]  P. Madesis, I. Ganopoulos, A. Anagnostis, and A. Tsaftaris, “The application of Bar-HRM (Barcode DNA-High Resolution Melting) analysis for authenticity testing and quantitative detection of bean crops (Leguminosae) without prior DNA purification,” Food Control, vol. 25, no. 2, pp. 576–582, 2012.
[50]  M. Y. Stoeckle, C. C. Gamble, R. Kirpekar, G. Young, S. Ahmed, and D. P. Little, “Commercial teas highlight plant DNA barcode identification successes and obstacles,” Scientific Reports, vol. 1, p. 42, 2011.
[51]  T. Hidayat, A. Pancoro, and D. Kusumawaty, “Utility of matK gene to assess evolutionary relationship of genus Mangifera (anacardiaceae) in Indonesia and Thailand,” Biotropia, vol. 18, no. 2, pp. 74–80, 2011.
[52]  J. Yu, H. X. Yan, Z. H. Lu, and Z. Q. Zhou, “Screening potential DNA barcode regions of chloroplast coding genome for citrus and its related genera,” Scientia Agricultura Sinica, vol. 44, no. 2, pp. 341–348, 2011.
[53]  T. Xin, H. Yao, H. Gao, et al., “Super food Lycium barbarum (Solanaceae) traceability via an internal transcribed spacer 2 barcode,” Food Research International, vol. 54, no. 2, pp. 1699–1704, 2013.
[54]  L. Jaakola, M. Suokas, and H. H?ggman, “Novel approaches based on DNA barcoding and high-resolution melting of amplicons for authenticity analyses of berry species,” Food Chemistry, vol. 123, no. 2, pp. 494–500, 2010.
[55]  R. L. Jarret, “DNA Barcoding in a crop genebank: the Capsicum annuum species complex,” Open Biology Journal, vol. 1, pp. 35–42, 2008.
[56]  S. Chen, H. Yao, J. Han et al., “Validation of the ITS2 region as a novel DNA barcode for identifying medicinal plant species,” PLoS ONE, vol. 5, no. 1, Article ID e8613, 2010.
[57]  T. Gao, H. Yao, J. Song et al., “Identification of medicinal plants in the family Fabaceae using a potential DNA barcode ITS2,” Journal of Ethnopharmacology, vol. 130, no. 1, pp. 116–121, 2010.
[58]  Y. Zuo, Z. Chen, K. Kondo, T. Funamoto, J. Wen, and S. Zhou, “DNA barcoding of panax species,” Planta Medica, vol. 77, no. 2, pp. 182–187, 2011.
[59]  V. A. Parvathy, V. P. Swetha, T. E. Sheeja, N. K. Leela, B. Chempakam, and B. Sasikumar, “DNA barcoding to detect chilli adulteration in traded black pepper powder,” Food Biotechnology, vol. 28, no. 1, pp. 25–40, 2014.
[60]  S. Federici, D. Fontana, A. Galimberti et al., “A rapid diagnostic approach to identify poisonous plants using DNA barcoding data,” Plant Biosystems. In press.
[61]  T. Hirao, S. Imai, H. Sawada, N. Shiomi, S. Hachimura, and H. Kato, “PCR method for detecting trace amounts of buckwheat (Fagopyrum spp.) in food,” Bioscience, Biotechnology and Biochemistry, vol. 69, no. 4, pp. 724–731, 2005.
[62]  I. Ganopoulos, P. Madesis, and A. Tsaftaris, “Universal ITS2 Barcoding DNA Region Coupled with High-Resolution Melting (HRM) Analysis for Seed Authentication and Adulteration Testing in Leguminous Forage and Pasture Species,” Plant Molecular Biology Reporter, vol. 30, no. 6, pp. 1322–1328, 2012.
[63]  I. Bosmali, I. Ganopoulos, P. Madesis, and A. Tsaftaris, “Microsatellite and DNA-barcode regions typing combined with High Resolution Melting (HRM) analysis for food forensic uses: a case study on lentils (Lens culinaris),” Food Research International, vol. 46, no. 1, pp. 141–147, 2012.
[64]  C. C. Ng, C. Y. Lin, W. S. Tzeng, C. C. Chang, and Y. T. Shyu, “Establishment of an internal transcribed spacer (ITS) sequence-based differentiation identification procedure for mei (Prunus mume) and plum (Prunus salicina) and its use to detect adulteration in preserved fruits,” Food Research International, vol. 38, no. 1, pp. 95–101, 2005.
[65]  I. Ganopoulos, C. Bazakos, P. Madesis, P. Kalaitzis, and A. Tsaftaris, “Barcode DNA high-resolution melting (Bar-HRM) analysis as a novel close-tubed and accurate tool for olive oil forensic use,” Journal of the Science of Food and Agriculture, vol. 93, no. 9, pp. 2281–2286, 2013.
[66]  M. Li, K. Au, H. Lam et al., “Identification of Baiying (Herba Solani Lyrati) commodity and its toxic substitute Xungufeng (Herba Aristolochiae Mollissimae) using DNA barcoding and chemical profiling techniques,” Food Chemistry, vol. 135, no. 3, pp. 1653–1658, 2012.
[67]  S. G. Newmaster, M. Grguric, D. Shanmughanandhan, S. Ramalingam, and S. Ragupathy, “DNA barcoding detects contamination and substitution in North American herbal products,” BMC Medicine, vol. 11, no. 1, p. 222, 2013.
[68]  B. Dhiman and M. Singh, “Molecular detection of Cashew Husk (Anacardium occidentale) adulteration in market samples of dry tea (Camellia sinensis),” Planta Medica, vol. 69, no. 9, pp. 882–884, 2003.
[69]  L. J. Wallace, S. M. A. L. Boilard, S. H. C. Eagle, J. L. Spall, S. Shokralla, and M. Hajibabaei, “DNA barcodes for everyday life: routine authentication of Natural Health Products,” Food Research International, vol. 49, no. 1, pp. 446–452, 2012.
[70]  M. A. Faria, A. Magalh?es, M. E. Nunes, and M. B. P. P. Oliveira, “High resolution melting of trnL amplicons in fruit juices authentication,” Food Control, vol. 33, no. 1, pp. 136–141, 2013.
[71]  M. Li, K. Wong, W. Chan et al., “Establishment of DNA barcodes for the identification of the botanical sources of the Chinese “cooling” beverage,” Food Control, vol. 25, no. 2, pp. 758–766, 2012.
[72]  J. Han, Y. Wu, W. Huang et al., “PCR and DHPLC methods used to detect juice ingredient from 7 fruits,” Food Control, vol. 25, no. 2, pp. 696–703, 2012.
[73]  A. Valentini, C. Miquel, and P. Taberlet, “DNA barcoding for honey biodiversity,” Diversity, vol. 2, no. 4, pp. 610–617, 2010.
[74]  A. Ortola-Vidal, H. Schnerr, M. Rojmyr, F. Lysholm, and A. Knight, “Quantitative identification of plant genera in food products using PCR and Pyrosequencing technology,” Food Control, vol. 18, no. 8, pp. 921–927, 2007.
[75]  M. Arleo, F. Ruibal, J. Pereyra, E. Miquel, M. Fernández, and C. Martínez, “A DNA-based approach to discriminate between quince and apple in quince jams,” International Food Research Journal, vol. 19, no. 4, pp. 1471–1477, 2012.
[76]  T. Yano, Y. Sakai, K. Uchida et al., “Detection of walnut residues in processed foods by polymerase chain reaction,” Bioscience, Biotechnology and Biochemistry, vol. 71, no. 7, pp. 1793–1796, 2007.
[77]  P. Madesis, I. Ganopoulos, I. Bosmali, and A. Tsaftaris, “Barcode High Resolution Melting analysis for forensic uses in nuts: a case study on allergenic hazelnuts (Corylus avellana),” Food Research International, vol. 50, no. 1, pp. 351–360, 2013.
[78]  G. Singh, Plant Systematics: an Integrated Approach, Science Publishers, New York, NY, USA, 2004.
[79]  H. Trindade, “Molecular biology of aromatic plants and spices. A review,” Flavour and Fragrance Journal, vol. 25, no. 5, pp. 272–281, 2010.
[80]  M. Viuda-Martos, Y. Ruiz-Navajas, J. Fernández-López, and J. A. Pérez-álvarez, “Spices as functional foods,” Critical Reviews in Food Science and Nutrition, vol. 51, no. 1, pp. 13–28, 2011.
[81]  A. Paton, M. R. Harley, and M. M. Harley, “Ocimum: an overview of classification and relationships,” in Basil: The Genus Ocimum, pp. 1–38, 1999.
[82]  A. O. Tucker, “The truth about mints,” Herb Companion, vol. 4, pp. 51–52, 1992.
[83]  V. Gobert, S. Moja, M. Colson, and P. Taberlet, “Hybridization in the section Mentha (Lamiaceae) inferred from AFLP markers,” American Journal of Botany, vol. 89, no. 12, pp. 2017–2023, 2002.
[84]  A. Torelli, M. Marieschi, and R. Bruni, “Authentication of saffron (Crocus sativus L.) in different processed, retail products by means of SCAR markers,” Food Control, vol. 36, no. 1, pp. 126–131, 2014.
[85]  K. Dhanya and B. Sasikumar, “Molecular marker based adulteration detection in traded food and agricultural commodities of plant origin with special reference to spices,” Current Trends in Biotechnology and Pharmacy, vol. 4, no. 1, pp. 454–489, 2010.
[86]  P. Posadzki, L. Watson, and E. Ernst, “Contamination and adulteration of herbal medicinal products (HMPs): an overview of systematic reviews,” European Journal of Clinical Pharmacology, vol. 69, no. 3, pp. 295–307, 2013.
[87]  M. Marieschi, A. Torelli, F. Poli, A. Bianchi, and R. Bruni, “Quality control of commercial Mediterranean oregano: development of SCAR markers for the detection of the adulterants Cistus incanus L., Rubus caesius L. and Rhus coriaria L.,” Food Control, vol. 21, no. 7, pp. 998–1003, 2010.
[88]  M. Marieschi, A. Torelli, A. Bianchi, and R. Bruni, “Detecting Satureja montana L. and Origanum majorana L. by means of SCAR-PCR in commercial samples of Mediterranean oregano,” Food Control, vol. 22, no. 3-4, pp. 542–548, 2011.
[89]  M. Marieschi, A. Torelli, A. Bianchi, and R. Bruni, “Development of a SCAR marker for the identification of Olea europaea L.: a newly detected adulterant in commercial Mediterranean oregano,” Food Chemistry, vol. 126, no. 2, pp. 705–709, 2011.
[90]  M. Barbuto, A. Galimberti, E. Ferri et al., “DNA barcoding reveals fraudulent substitutions in shark seafood products: the Italian case of “palombo” (Mustelus spp.),” Food Research International, vol. 43, no. 1, pp. 376–381, 2010.
[91]  Z. Hubalkova and E. Rencova, “One-step multiplex PCR method for the determination of pecan and Brazil nut allergens in food products,” Journal of the Science of Food and Agriculture, vol. 91, no. 13, pp. 2407–2411, 2011.
[92]  J. Costa, I. Mafra, I. Carrapatoso, and M. B. P. P. Oliveira, “Almond allergens: molecular characterization, detection, and clinical relevance,” Journal of Agricultural and Food Chemistry, vol. 60, no. 6, pp. 1337–1349, 2012.
[93]  F. M. Hammouda, A. M. Rizk, M. M. El-Missiry et al., “Poisonous plants contaminating edible ones and toxic substances in plant foods. IV. Phytochemistry and toxicity of Lolium temulentum,” International Journal of Crude Drug Research, vol. 26, no. 4, pp. 240–245, 1988.
[94]  R. Walker, “Criteria for risk assessment of botanical food supplements,” Toxicology Letters, vol. 149, no. 1–3, pp. 187–195, 2004.
[95]  M. L. Colombo, F. Assisi, T. D. Puppa et al., “Most commonly plant exposures and intoxications from outdoor toxic plants,” Journal of Pharmaceutical Sciences and Research, vol. 2, no. 7, pp. 417–425, 2010.
[96]  Y. Finkelstein, S. E. Aks, J. R. Hutson et al., “Colchicine poisoning: the dark side of an ancient drug,” Clinical Toxicology, vol. 48, no. 5, pp. 407–414, 2010.
[97]  M. A. Berdai, S. Labib, K. Chetouani, and M. Harandou, “Atropa Belladonna intoxication: a case report,” Pan African Medical Journal, vol. 11, p. 72, 2012.
[98]  E. R?der, “Medicinal plants in Europe containing pyrrolizidine alkaloids,” Pharmazie, vol. 50, no. 2, pp. 83–98, 1995.
[99]  C. Franz, R. Chizzola, J. Novak, and S. Sponza, “Botanical species being used for manufacturing plant food supplements (PFS) and related products in the EU member states and selected third countries,” Food and Function, vol. 2, no. 12, pp. 720–730, 2011.
[100]  H. Wiedenfeld and J. Edgar, “Toxicity of pyrrolizidine alkaloids to humans and ruminants,” Phytochemistry Reviews, vol. 10, no. 1, pp. 137–151, 2011.
[101]  K. S. Burgess, A. J. Fazekas, P. R. Kesanakurti et al., “Discriminating plant species in a local temperate flora using the rbcL+matK DNA barcode,” Methods in Ecology and Evolution, vol. 2, no. 4, pp. 333–340, 2011.
[102]  A. Sandionigi, A. Galimberti, M. Labra et al., “Analytical approaches for DNA barcoding data-how to find a way for plants?” Plant Biosystems, vol. 146, no. 4, pp. 805–813, 2012.
[103]  S. Ratnasingham and P. D. N. Hebert, “BOLD: the barcode of life data system: barcoding,” Molecular Ecology Notes, vol. 7, no. 3, pp. 355–364, 2007.
[104]  F. De Mattia, R. Gentili, I. Bruni et al., “A multi-marker DNA barcoding approach to save time and resources in vegetation surveys,” Botanical Journal of the Linnean Society, vol. 169, no. 3, pp. 518–529, 2012.
[105]  M. L. Kuzmina, K. L. Johnson, H. R. Barron, and P. D. N. Hebert, “Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library,” BMC Ecology, vol. 12, p. 25, 2012.
[106]  F. Sanger, S. Nicklen, and A. R. Coulson, “DNA sequencing with chain-terminating inhibitors,” Proceedings of the National Academy of Sciences of the United States of America, vol. 74, no. 12, pp. 5463–5467, 1977.
[107]  M. Hajibabaei, S. Shokralla, X. Zhou, G. A. C. Singer, and D. J. Baird, “Environmental barcoding: a next-generation sequencing approach for biomonitoring applications using river benthos,” PLoS ONE, vol. 6, no. 4, Article ID e17497, 2011.
[108]  S. Shokralla, J. L. Spall, J. F. Gibson, and M. Hajibabaei, “Next-generation sequencing technologies for environmental DNA research,” Molecular Ecology, vol. 21, no. 8, pp. 1794–1805, 2012.
[109]  M. L. Metzker, “Sequencing technologies—the next generation,” Nature Reviews Genetics, vol. 11, no. 1, pp. 31–46, 2010.
[110]  M. L. Coghlan, J. Haile, J. Houston et al., “Deep sequencing of plant and animal DNA contained within traditional Chinese medicines reveals legality issues and health safety concerns,” PLoS Genetics, vol. 8, no. 4, Article ID e1002657, 2012.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133